Search Results (537)

Bayberry (Morella rubra Lour.; syn. Myrica rubra (Lour.) Siebold & Zucc.) leaves are rich in bioactive compounds but remain underutilized. This study investigated the optimal harvest stage and processing methods to develop high-quality functional powder. We first compared three growth stages: red buds (RB), new leaves (NL), and old leaves (OL). RB exhibited the highest antioxidant capacity and unique volatile profile; however, NL was selected for processing optimization due to the balance between quality and biomass availability. Subsequently, NL was subjected to freeze-drying (FD), mechanical drying (MD), steaming followed by MD (S-MD), and shade drying (SD). Results showed that FD preserved the vibrant green color, glandular trichome structure, ascorbic acid, and fresh volatiles (monoterpenes). Conversely, thermal drying (MD and S-MD) disrupted cellular barriers, which facilitated the extraction of minerals and robust polyphenols like myricitrin, yielding the highest extraction of flavonoids and corresponding antioxidant activity, measured by hydrophilic oxygen radical absorbance capacity (H-ORAC), in hot water extracts than FD. SD significantly degraded quality due to prolonged enzymatic oxidation. While FD is ideal for preserving aesthetics and heat-sensitive nutrients, low-cost MD and S-MD are recommended for producing antioxidant-rich powders for functional food applications where extraction efficiency is prioritized. Full article

The rapid expansion of the poultry industry has led to the large-scale generation of feather waste, creating serious environmental and public health concerns due to the recalcitrant nature of keratin. Poultry feathers are composed mainly of highly cross-linked keratin proteins stabilized by numerous disulfide bonds, which confer resistance to conventional proteolytic enzymes and natural degradation processes. This review examines the potential of keratinolytic fungi and their enzymes as sustainable, eco-friendly, and value-added strategies for poultry feather waste management and resource recovery. It discusses the environmental and health risks associated with improper feather disposal, such as pathogen proliferation, odor generation, and ecosystem contamination. Conventional management approaches, steam pressure hydrolysis, mechanical grinding, thermal treatment, acid–alkali hydrolysis, and oxidation, are critically evaluated in terms of efficiency and environmental impact. The review further highlights biological degradation pathways mediated by keratinolytic fungi and enzymes, with emphasis on fungal genera such as Aspergillus and Chrysosporium. Key mechanisms of fungal keratin degradation, including sulfitolysis, proteolysis, deamination, hyphal penetration, enzyme secretion, and biofilm formation, are discussed. Finally, industrial, agricultural, and feed applications of keratinases, along with advances in strain improvement, omics technologies, synthetic biology, and associated biosafety and regulatory considerations, are addressed. Full article

Increasing global demand for animal-based protein has created a critical environmental management challenge regarding manure accumulation in intensive livestock production. Gasification offers a sustainable solution by converting organic residues into renewable synthetic gas (syngas) and carbon-rich biochar. This study systematically evaluated the performance of three major types of animal waste—dairy manure, poultry litter, and swine manure—against a lignocellulosic control (wood veneer waste) in a top-lit updraft (TLUD) gasifier. Three airflow rates (10, 15, and 20 L min⁻¹) were studied. The results indicated that increasing airflow significantly elevated the gasifier flame front temperatures, with poultry litter achieving the highest peak temperature (825.5 °C), followed by swine manure and dairy manure (753.7 and 727.0 °C, respectively) at 20 L min⁻¹ airflow. While dairy manure exhibited the fastest linear burning rate (25.7 mm/min), poultry litter demonstrated the highest mass consumption rate (32.8 g/min). Feedstock chemistry drove distinct reaction pathways in syngas composition. Poultry litter emerged as the superior feedstock for H₂ production, achieving a peak H₂ concentration of 10.78% at 20 L min⁻¹, which attributed to a synergistic combination of outstanding temperature, moisture content and catalytic alkali metals that promoted steam reforming and water–gas shift reactions. CO production was dominated by wood veneer (17.6%), which was driven by the dominance of elemental carbon and fixed solid (FS) content that favored partial oxidation and a Boudouard reaction. These findings suggest that while airflow regulates thermal kinetics, the specific energy profile of the produced syngas is fundamentally determined by the physiochemical properties of the biomass precursor. Full article

Linear alkylbenzene (LAB) is the main raw material used to make biodegradable detergents, and its production process is based on aromatic alkylation. HY zeolites that have undergone controlled dealumination and desilication have led industrial standards amongst solid acid catalysts because of their controllable acidity and hierarchical pore structure. Coke formation in such systems can assume a dual role, which is dependent on its condition. Though the over-deposition is known to cause deactivation by blocking the micropores, Bronsted acid-site masking, and diffusion collapse, the low-level deposition could also be done to increase the monoalkylate selectivity by the pore mouth catalysis, steric modulation, and selective suppression of secondary alkylation pathways. The critical review is done on the structural-kinetic interaction that determines the coke evolution in HY-based catalysts. In order to moderate the acid-site density and enhance hydrothermal stability, dealumination (Si/Al optimization of about 2.5 to 30–100) occurs, but to reduce deep-pore coke formation, desilication (interconnected mesopores) is created. The bimodal porosity and regulated acidity are found to be synergistic, as hierarchical HY zeolites produced through successive cycles of steam and alkaline treatments not only show LAB selectivity in excess of 90% but also exhibit much longer catalyst lifetimes. Quantitative research on the beneficial coke regime revealed that it was composed of about 36 wt% hydrogen-rich species, which were localized at the pore mouths, hence enhancing monoalkylation selectivity by 15–40%. Beyond a critical transition window (e.g., 8–12 wt.%), coke formation to condensed polyaromatic and graphitic products leads to fast deactivated coke formation, which is due to percolation limits and transport-controlled kinetics. More advanced techniques of characterization of the coke, e.g., temperature-programmed oxidation (TPO), ²⁷Al MAAS NMR, and UV-Raman spectroscopy, indicate how the coke is changed to highly structured graphitic deposits of high oxidation activation energy. Activity recovery of 85–98% is obtained in regeneration processes, including controlled oxidative calcination, microwave-based and plasma-based processes, and thermal management protocols, and it would be determined by the chemistry of the coke, its spatial distribution, and the regeneration protocols. This paper has developed a mechanistic coke control system by cross-tuning the acidity and development of an effective pore network, which led to a sustainable aromatic alkylation reaction with minimal activity loss, high selectivity, and long life. Full article

Changes in lifestyle and food consumption patterns have contributed to a growing demand for home meal replacements (HMRs), emphasizing the need for high-quality seafood-based products. This study aimed to develop a grilled Pacific cod (Gadus macrocephalus) fillet HMR prototype and to evaluate optimal processing conditions, quality characteristics, and shelf-life stability. High-frequency thawing was selected to improve raw material handling by minimizing drip loss to 11.91% and reducing thawing time to 15 min. A thyme-based marinade at a concentration of 3% for 20 min was applied to reduce odor and enhance sensory quality, and superheated steam grilling was compared with conventional heating methods. Processing parameters were optimized using response surface methodology, and smoking conditions were evaluated using different wood types. Superheated steam grilling produced superior sensory attributes under optimal conditions of 340 °C for 4 min, followed by cherry wood smoking at 60 °C for 5 min. The combined processing approach reduced total bacterial counts while maintaining acceptable physicochemical quality characteristics. Thermal processing increased texture firmness and nutritional density due to moisture loss, reduced lipid oxidation, and modified amino acid and fatty acid profiles. Shelf-life modeling indicated safe storage for up to 18 months under frozen conditions. These findings demonstrate that integrated marination, superheated steam grilling, and controlled smoking can be effectively applied to produce a safe, stable, and high-quality grilled Pacific cod HMR product. Full article

Biomass chemical looping gasification coupled with CO₂ splitting (BCLGCS) presents a promising carbon-negative route for simultaneous syngas production and CO₂ utilization, where the selection of oxygen carriers (OCs) is critical. Compared to single-metal oxides, composite metal OCs offer thermodynamic advantages. This study aims to evaluate the thermodynamic performance of composite metal OCs (LaFeO₃, BaFeO₃, CaFe₂O₄, and Ca₂Fe₂O₅) in BCLGCS to overcome the thermodynamic limitations of conventional biomass-CO₂ gasification. Gibbs free energy minimization calculations were performed to predict gas compositions and oxygen carrier phase transformations under varying operating conditions. Results show that steam addition promotes gasification by increasing H₂ content and lowering required temperatures, but substantially reduces CO₂ conversion in the splitting reactor by consuming residual char. Ca₂Fe₂O₅ demonstrates superior adaptability with tunable H₂/CO ratios, while LaFeO₃ requires high OC loading and BaFeO₃ undergoes deactivation via BaCO₃ formation. This work reveals inherent thermodynamic conflicts between gasification and CO₂ splitting steps, indicating that the optima for syngas production and CO₂ utilization are mutually exclusive, an insight not previously quantified in BCLGCS literature. The findings provide theoretical guidance for designing carbon-tolerant OCs and optimizing process parameters, advancing BCLGCS toward practical carbon-negative applications. Full article

Water is a critical resource underpinning natural, societal and economic development, and its importance will grow bigger in the next decades. Interfacial solar evaporators are a promising and cost-effective technology for the generation of freshwater from saline and polluted waters. Yet, although these devices effectively reject salts and non-volatile pollutants, the presence of volatile organic compounds in the water source may lead to low water quality of the distillate. This review addresses the introduction of photocatalytic materials in solar evaporator devices to improve water quality, highlighting in particular possible synergies and incompatibilities between the materials promoting these functionalities. The interactions of the photocatalyst with photothermal materials are described, along with an overview of the materials most commonly selected for both functionalities. A positive interaction clearly emerges, with the photothermal materials not only accelerating evaporation but also generally stimulating the photocatalytic degradation of VOCs. Limits to the implementation of such a combination are described, including those due to electrolyte content and salt accumulation, reaction rate and mass transfer. Finally, recommendations regarding testing conditions and future studies are presented. Full article

The conventional treatment of high-concentration volatile organic compounds (VOCs) relies on energy-intensive dilution to avoid explosion risks. This study proposes an efficient catalytic combustion process treating VOCs directly within the explosive range while recovering reaction heat using Pt/γ-Al₂O₃-based catalysts promoted with La and Ce. Catalysts (0.05–0.5 wt% Pt) were synthesized via impregnation and characterized using FE-SEM, BET, and XRD. Catalytic combustion experiments at VOC concentrations up to 13,000 ppm showed combustion initiation below 200 °C, achieving 83–99% conversions at 300 °C with complete oxidation to CO₂. Although 5 vol.% moisture significantly inhibited low-temperature activity through competitive adsorption, La and Ce promoters (10 wt%) effectively overcame this limitation by increasing surface area (up to 194.93 m²/g) and oxygen mobility. The Ce-promoted catalyst demonstrated superior water tolerance, achieving complete conversion at 200–210 °C due to its high Oxygen Storage Capacity (OSC). Bench-scale validation using a 1 Nm³/h system confirmed industrial feasibility. Operating at 220 °C with 13,000 ppm toluene for 100 h, the catalyst maintained >99.98% conversion with negligible deactivation and THC emissions below 2 ppm. The double-jacket heat exchanger effectively managed reaction heat (limiting temperature rise to ~20 °C) and recovered it as steam. Compared to Regenerative Thermal Oxidation, this Regenerative Catalytic Oxidation approach reduced emissions and energy consumption. This work demonstrates a robust “combustion-with-recovery” strategy for high-concentration VOC treatment, offering a sustainable alternative with high efficiency, stability, and safe energy-integrated operation. Full article

The Mixed-Conduction Model for oxide films is used to quantitatively interpret in situ electrochemical and ex situ surface analytical results on the corrosion of AISI 316L (an internal reactor material) and Alloy 690 (a steam generator tube material) in small modular reactor primary coolant with the addition of soluble Zn. The model parameters of alloy oxidation and corrosion release are estimated with the time of exposure up to 168 h and anodic polarization potential (up to −0.25 V vs. standard hydrogen electrode) using fitting of the transfer function to experimental impedance spectra. Model parameters of individual alloy constituents are estimated by fitting of the model equations to the atomic fraction profiles of respective elements in the formed oxide obtained by Glow-Discharge Optical Emission Spectroscopy (GDOES). Conclusions on the effect of Zn addition on film growth and cation release processes in boron-free SMR coolant are drawn and future research directions are outlined. Full article

The aims of this study were to evaluate the impact of probiotics (added as a starter sourdough and microcapsules) on gluten-free (GF) rice–amaranth steamed bread (SB) regarding physicochemical characteristics, sensory attributes, probiotic viability, and volatile organic compounds (VOCs). Also, probiotic viability, pH, total titratable acidity (TTA), moisture content, water activity, and texture were determined for 10 days of storage. GF-SB based on rice and amaranth was formulated and cooked at 90 ± 2 °C for 40 min. Three types of GF-SB were studied: control, with 30% sourdough fermented using Lactiplantibacillus plantarum NRRL B-4496 (GF-P), and with sourdough and encapsulated Limosilactobacillus reuteri DSM 17938 (GF-PC). The encapsulation yield was 94.9%. The viability of both probiotics was drastically reduced after steamed cooking, with losses ranging from 6 to 8 log₁₀ CFU/g. Sourdough decreased the pH (from 6.04 to 5.48–5.71) and hardness (control 46 N, sourdough ~25 N) while increasing lactic and acetic acids, moisture content (control 38%, sourdough ~46%), and water activity. Sourdough and probiotic capsules did not affect volume (~1.24 cm³/g), width-to-height ratio (~2.4), color, or sensory attributes. The VOCs revealed higher relative abundances of certain yeast-derived higher alcohols and oxidation-related carbonyl-trapping derivatives in control GF-SB, whereas bread with sourdough showed higher levels of long-chain hydrocarbons and esters, such as heptacosane and decanoic acid decyl ester. During the storage, Lpb. plantarum increased to ~3 log₁₀ CFU/g and Lim. reuteri remained steady. pH and TTA (0.03–0.04%) remained constant during storage. After 10 days of storage, hardness increased significantly (p < 0.05) in all GF-SB, doubling the initial values. Moisture content remained constant, while water activity decreased in GF-P (Δ = 0.025) and the control (Δ = 0.015). The use of sourdough in GF-SB improved texture, moisture content, and VOCs without modifying physical and sensory properties. Full article

Nanoparticle-mediated photothermal conversion exploits the unique light-to-heat transduction properties of engineered nanomaterials to address challenges in energy, water, and healthcare. This review first examines fundamental mechanisms—localized surface plasmon resonance (LSPR) in plasmonic metals and broadband interband transitions in semiconductors—demonstrating how tailored nanoparticle compositions can achieve >96% absorption across 250–2500 nm and photothermal efficiencies exceeding 98% under one-sun illumination (1000 W·m⁻², AM 1.5G). Next, we highlight advances in solar steam generation and desalination: floating photothermal receivers on carbonized wood or hydrogels reach >95% efficiency in solar-to-vapor conversion and >2 kg·m⁻²·h⁻¹ evaporation rates; three-dimensional architectures recapture diffuse flux and ambient heat; and full-spectrum nanofluids (LaB₆, Au colloids) extend photothermal harvesting into portable, scalable designs. We then survey photothermal-enhanced thermal energy storage: metal-oxide–paraffin composites, core–shell phase-change material (PCM) nanocapsules, and MXene– polyethylene glycol—PEG—aerogels deliver >85% solar charging efficiencies, reduce supercooling, and improve thermal conductivity. In biomedicine, gold nanoshells, nanorods, and transition-metal dichalcogenide (TMDC) nanosheets enable deep-tissue photothermal therapy (PTT) with imaging guidance, achieving >94% tumor ablation in preclinical and pilot clinical studies. Multifunctional constructs combine PTT with chemotherapy, immunotherapy, or gene regulation, yielding synergistic tumor eradication and durable immune responses. Finally, we explore emerging opto-thermal nanobiosystems—light-triggered gene silencing in microalgae and poly(N-isopropylacrylamide) (PNIPAM)–gold nanoparticle (AuNP) membranes for microfluidic photothermal filtration and control—demonstrating how nanoscale heating enables remote, reversible biological and fluidic functions. We conclude by discussing challenges in scalable nanoparticle synthesis, stability, and integration, and outline future directions: multicomponent high-entropy alloys, modular photothermal–PCM devices, and opto-thermal control in synthetic biology. These interdisciplinary innovations promise sustainable solutions for global energy, water, and healthcare demands. Full article

This study investigates the oxidative steam reforming (OSR) of simulated bio-oil aqueous fractions using Co/CeO₂-SBA-15 catalysts. Five representative compounds—methanol, acetic acid, hydroxyacetone, phenol, and furfural—were evaluated to assess their reactivity for hydrogen production. Aliphatic compounds achieved nearly complete conversion and stable hydrogen yields, while aromatic structures led to lower conversion and higher coke formation. Furfural exhibited higher reactivity than phenol due to its furan ring and aldehyde group. Catalysts with 10 and 20 wt.% Ce showed similar activity, but Co/20CeO₂-SBA-15 presented lower hydrogen yield. For this reason, next experiments of OSR of model compound mixtures were carried out only with Co/10CeO₂-SBA-15. To approach real bio-oil complexity, ternary and quinary mixtures were tested. High conversion and hydrogen yield were maintained over 50 h when the ternary mixture (methanol, hydroxyacetone, and acetic acid) was fed. When the quinary mixture was used as feedstock, which includes furfural and phenol, lower conversions were obtained for these compounds compared to aliphatic ones, although conversions remained above 80% after 50 h (88.9% for furfural and 82.6% for phenol). These results highlight Co/10CeO₂-SBA-15 as a viable catalyst for bio-oil aqueous fraction valorization under OSR conditions. Full article

CO₂ valorization from real feedstocks through CH₄ tri-reforming (CH₄-TR), combining steam reforming (SR), dry reforming (DR), and partial oxidation (CPO) of methane in a single process, is a desirable strategy for greenhouse gas mitigation and syngas (CO + H₂) production. NiCo/γ−Al₂O₃ catalysts prepared by impregnation at different relative metal contents (Ni₅₀Co₅₀ and Ni₃₀Co₇₀) were investigated for CH₄-TR in a fixed-bed reactor under conventional heating and characterized by XRD, FESEM, and Raman spectroscopy after catalytic runs. This study focused on the role of the Ni/Co ratio and feed composition on selectivity for CO₂ valorization, syngas yield, and deactivation resistance. Both the catalysts showed high activity, with a superior performance of Ni₅₀Co₅₀ confirming Ni metal species as the active sites. While in DR, a slow deactivation occurred due to coke deposition, in CH₄-TR, the addition of small O₂ and/or H₂O amounts stabilized activity and selectivity due to surface carbon removal. Large O₂ and H₂O amounts strongly inhibited CO₂ conversion due to competition with CPO and SR, in the order CPO ≥ DR > SR. Interestingly, the stoichiometric CH₄-to-oxidants ratio favored the DR pathway, giving very high CO₂ conversion. Modulating CH₄ addition into real flue mixtures renders CH₄-TR on NiCo/γ-Al₂O₃ catalysts a favorable strategy for effective valorization of CO₂ industrial or biomass-derived streams. Full article

An ethnobotanical survey in the northern mountainous region of Vietnam identified four Elsholtzia species, E. blanda, E. ciliata, E. communis, and E. penduliflora, growing naturally above 1500 m and traditionally used by local ethnic communities to treat skin-related ailments. This study investigates their essential oil possible chemotypes, antimicrobial properties, and potential mechanisms of action through molecular docking. Essential oils obtained by steam distillation were analyzed using GC–MS. E. blanda (yield 1.17%) was characterized by high levels of 1,8-cineole (29.0%) and camphor (17.0%). E. ciliata (1.02%) represented a possible limonene-dominant chemotype (71.0%). E. communis (1.91%) contained an exceptionally high proportion of rosefuran oxide (86.2%), whereas E. penduliflora (0.91%) exhibited a pronounced 1,8-cineole chemotype (92.1%). All essential oils showed antimicrobial activity against Staphylococcus aureus (MSSA and MRSA), Escherichia coli, and Candida albicans, with MIC values ranging from 0.4% to 3.2%. Except for E. ciliata against C. albicans, MBC/MIC and MFC/MIC ratios ≤ 4 indicated predominantly bactericidal or fungicidal effects. Molecular docking further identified nine of twenty-eight detected constituents as strong binders to microbial target proteins. These findings expand current knowledge on possible chemotypic diversity within the genus, particularly the discovery of a high-altitude limonene chemotype in E. ciliata and the identification of E. penduliflora as a rich natural source of 1,8-cineole. The convergence of chemical, biological, and in silico evidence supports the ethnomedicinal relevance of Elsholtzia species and highlights their potential as candidates for developing natural antimicrobial agents. Full article

Improving the energy efficiency of advanced ultra-supercritical (USC) power plants by increasing steam operating temperature up to 700 °C can be achieved, at reduced cost, by using novel engineering design concepts, such as coated steam pipe systems manufactured from high temperature materials commonly used in current operational power plants. The durability of thermal barrier coatings (TBC) in advanced USC coal power systems is critically influenced by thermally grown oxide (TGO) evolution and interfacial stress under thermo-chemo-mechanical coupling. This study investigates a novel dual-pipe coating system comprising an inner P91 steel pipe with dual coatings and external cooling, designed to mitigate thermal mismatch stresses while operating at 700 °C. A finite element framework integrating thermo-chemo-mechanical coupling theory is developed to analyze TGO growth kinetics, oxygen diffusion, and interfacial stress evolution. Results reveal significant thermal gradients across the coating, reducing the inner pipe surface temperature to 560 °C under steady-state conditions. Oxygen diffusion and interfacial curvature drive non-uniform TGO thickening, with peak regions exhibiting 23% greater thickness than troughs after 500 h of oxidation. Stress analysis identifies axial stress dominance at top coat/TGO and TGO/bond coat interfaces, increasing from 570 MPa to 850 MPa due to constrained volumetric changes and incompatible growth strains. The parabolic TGO growth kinetics and stress redistribution mechanisms underscore the critical role of thermo-chemo-mechanical interactions in interfacial degradation. These research findings will facilitate the optimization of coating architectures and the enhancement of structural integrity in high-temperature energy systems. Meanwhile, clarifying the stress evolution within the coating can improve the ability to predict failures in USC coal power technology. Full article